Religious labels and food preferences, but not country of origin, support opposing face aftereffects.

Face templates can be experimentally manipulated, and category-contingent aftereffects suggest discrete templates across social groups. We tested whether 1) explicit religious labels, 2) food preferences, and 3) country of origin would support religion-contingent aftereffects across Christians and Muslims face sets. While viewing face images, ninety-three participants heard audio that stated either 1) a character's religious identity, 2) preferred food, or 3) country of origin. Participants viewed contracted Christian faces and expanded Muslim faces during the training phase. To measure adaptation, before and after the training phases, participants selected the face out of a pair of expanded and contracted Christian or Muslim faces that they found more attractive. Contingent aftereffects were found in the religious explicit (t(30) = 2.49, p = 0.02, Cohen's d = 0.58) and food conditions (t(30) = -3.77, p < 0.01, Cohen's d = -0.82), but not the country condition (t(30) = 1.64, p = 0.11, Cohen's d = 0.31). This suggests that religious labels and food preferences create socially meaningful groups, but country of origin does not. This is evidence of an impact of social categorization on visual processing.

(Don't) look where you are going: Evidence for a travel direction signal in humans that is independent of head direction.

We often assume that travel direction is redundant with head direction, but from first principles, these two factors provide differing spatial information. Although head direction has been found to be a fundamental component of human navigation, it is unclear how self-motion signals for travel direction contribute to forming a travel trajectory. Employing a novel motion adaptation paradigm from visual neuroscience designed to preclude a contribution of head direction, we found high-level aftereffects of perceived travel direction, indicating that travel direction is a fundamental component of human navigation. Interestingly, we discovered a higher frequency of reporting perceived travel toward the adapted direction compared to a no-adapt control-an aftereffect that runs contrary to low-level motion aftereffects. This travel aftereffect was maintained after controlling for possible response biases and approaching effects, and it scaled with adaptation duration. These findings demonstrate the first evidence of how a pure travel direction signal might be represented in humans, independent of head direction. (PsycInfo Database Record (c) 2024 APA, all rights reserved).

A category contingent aftereffect for faces labelled with different religious affiliation is seen 7 days after adaptation.

Visual adaptation occurs after a prolonged exposure to a stimulus. The duration of aftereffects differs across stimuli type, and face aftereffects may be especially long lasting. The current study investigates adaptation decay of category contingent opposing aftereffects. Specifically, we tested whether naïve undergraduate participants' adaptation to photos of faces with explicit religious labels, differed from that of participants who had adapted to the same faces 7 days previously. We also tested whether 7-day old category-contingent opposing aftereffects interfere with the ability to re-adapt to a new condition. In Session 1, undergraduates made attractiveness preference selections before and after adapting to two groups of distorted faces. Participants then returned 7 days later to re-assess the attractiveness of the same faces. Participants were then adapted to the two groups of faces distorted in the opposite direction. Adaptation strength was stronger in Session 1 than in Session 2, although adaptation strength was not related to pre-adaptation selections. Week-old aftereffects interfered with the creation of aftereffects in the opposite direction 7 days later.

Frequency of adapting events affects face aftereffects but not blur aftereffects.

The dynamics of visual adaptation remain poorly understood. Recent studies have found that the strength of adaptation aftereffects in the perception of numerosity depends more strongly on the number of adaptation events than on the duration of the adaptation. We investigated whether such effects can be observed for other visual attributes. We measured blur (perceived focus-sharp vs blurred adapt) and face (perceived race- Asian vs. White adapt) aftereffects by varying the number of adaptation events (4 or 16) and the duration of each adaptation event (0.25 s or 1 s). We found evidence for an effect of event number on face but not on blur adaptation, though the effect for faces was significant for only one of the two face adapt conditions (Asian). Our results suggest that different perceptual dimensions may vary in how adaptation effects accrue, potentially because of differences in factors such as the sites (early or late) of the sensitivity changes or nature of the stimulus. These differences may impact how and how rapidly the visual system can adjust to different visual properties.

Object Image Size Is a Fundamental Coding Dimension in Human Vision: New Insights and Model.

In previous psychophysical work we found that luminance contrast is integrated over retinal area subject to contrast gain control. If different mechanisms perform this operation for a range of superimposed retinal regions of different sizes, this could provide the basis for size-coding. To test this idea we included two novel features in a standard adaptation paradigm to discount more pedestrian accounts of repulsive size-aftereffects. First, we used spatially jittering luminance-contrast adaptors to avoid simple contour displacement aftereffects. Second, we decoupled adaptor and target spatial frequency to avoid the well-known spatial frequency shift aftereffect. Empirical results indicated strong evidence of a bidirectional size adaptation aftereffect. We show that the textbook population model is inappropriate for our results, and develop our existing model of contrast perception to include multiple size mechanisms with divisive surround-suppression from the largest mechanism. For a given stimulus patch, this delivers a blurred step-function of responses across the population, with contrast and size encoded by the height and lateral position of the step. Unlike for textbook population coding schemes, our human results (N = 4 male, N = 4 female) displayed two asymmetries: (i) size aftereffects were greatest for targets smaller than the adaptor, and (ii) on that side of the function, results did not return to baseline, even when targets were 25% of adaptor diameter. Our results and emergent model properties provide evidence for a novel dimension of visual coding (size) and a novel strategy for that coding, consistent with previous results on contrast detection and discrimination for various stimulus sizes.

Tilt aftereffect spreads across the visual field.

The tilt aftereffect (TAE) is observed when adaptation to a tilted contour alters the perceived tilt of a subsequently presented contour. Thus far, TAE has been treated as a local aftereffect observed only at the location of the adapter. Whether and how TAE spreads to other locations in the visual field has not been systematically studied. Here, we sought an answer to this question by measuring TAE magnitudes at locations including but not limited to the adapter location. The adapter was a tilted grating presented at the same peripheral location throughout an experimental session. In a single trial, participants indicated the perceived tilt of a test grating presented after the adapter at one of fifteen locations in the same visual hemifield as the adapter. We found non-zero TAE magnitudes in all locations tested, showing that the effect spreads across the tested visual hemifield. Next, to establish a link between neuronal activity and behavioral results and to predict the possible neuronal origins of the spread, we built a computational model based on known characteristics of the visual cortex. The simulation results showed that the model could successfully capture the pattern of the behavioral results. Furthermore, the pattern of the optimized receptive field sizes suggests that mid-level visual areas, such as V4, could be critically involved in TAE and its spread across the visual field.

Opposing aftereffects between a White male face set and a diverse face set.

Opposing aftereffects have been observed for faces categorized by gender, race, and age. In order to form opposing aftereffects, it appears that the two face sets must be both physically distinct and differ in terms of social meaning. The current study tests whether (1) a face set that is diverse with respect to sex and race can produce a coherent aftereffect and (2) whether this diversity itself is socially meaningful enough to support opposing aftereffects. Participants adapted to a homogenous face set consisting of only White male Republican congressmen and a diverse face set consisting of White, Asian, Black, and Latino male and female Democratic congress members. Opposing aftereffects were observed: participants adapted simultaneously and in opposite directions to the face sets. These results are the first evidence of adaptation to a face set that varies based on race and sex, and the first evidence of diversity being perceived as a socially meaningful category marker.

Temporal dynamics of face adaptation.

The appearance of a face can be strongly affected by adaptation to faces seen previously. A number of studies have examined the time course of these aftereffects, but the integration time over which adaptation pools signals to control the adaptation state remains uncertain. Here we examined the effects of temporal frequency on face gender aftereffects induced by a pair of faces alternating between the two genders to assess when the aftereffects were pooled over successive faces versus driven by the last face seen. In the first experiment, we found that temporal frequencies between 0.25 and 2.00 Hz all failed to produce an aftereffect, suggesting a fairly long integration time. In the second experiment, we therefore probed slower alternation rates of 0.03 to 0.25 Hz. A rate of 0.0625 Hz (i.e., 8 seconds per face) was required to generate significant aftereffects from the last presented face and was consistent with an average time constant of 15 to 20 seconds for an exponentially decaying integration window. This integration time is substantially longer than found previously for analogous effects for alternating colors, and thus points to a potentially slower mechanism of adaptation for faces compared with chromatic adaptation.

The aftereffect of the ensemble average of facial expressions on subsequent facial expression recognition.

An ensemble or statistical summary can be extracted from facial expressions presented in different spatial locations simultaneously. However, how such complicated objects are represented in the mind is not clear. It is known that the aftereffect of facial expressions, in which prolonged viewing of facial expressions biases the perception of subsequent facial expressions of the same category, occurs only when a visual representation is formed. Using this methodology, we examined whether an ensemble can be represented with visualized information. Experiment 1 revealed that the presentation of multiple facial expressions biased the perception of subsequent facial expressions to less happy as much as the presentation of a single face did. Experiment 2 compared the presentation of faces comprising strong and weak intensities of emotional expressions with an individual face as the adaptation stimulus. The results indicated that the perceptual biases were found after the presentation of four faces and a strong single face, but not after the weak single face presentation. Experiment 3 employed angry expressions, a distinct category from the test expression used as an adaptation stimulus; no aftereffect was observed. Finally, Experiment 4 clearly demonstrated the perceptual bias with a higher number of faces. Altogether, these results indicate that an ensemble average extracted from multiple faces leads to the perceptual bias, and this effect is similar in terms of its properties to that of a single face. This supports the idea that an ensemble of faces is represented with visualized information as a single face.

Experience-dependent reshaping of body gender perception.

Protracted exposure to specific stimuli causes biased visual aftereffects at both low- and high-level dimensions of a stimulus. Recently, it has been proposed that alterations of these aftereffects could play a role in body misperceptions. However, since previous studies have mainly addressed manipulations of body size, the relative contribution of low-level retinotopic and/or high-level object-based mechanisms is yet to be understood. In three experiments, we investigated visual aftereffects for body-gender perception, testing for the tuning of visual aftereffects across different characters and orientation. We found that exposure to a distinctively female (or male) body makes androgynous bodies appear as more masculine (or feminine) and that these aftereffects were not specific for the individual characteristics of the adapting body (Exp.1). Furthermore, exposure to only upright bodies (Exp.2) biased the perception of upright, but not of inverted bodies, while exposure to both upright and inverted bodies (Exp.3) biased perception for both. Finally, participants' sensitivity to body aftereffects was lower in individuals with greater communication deficits and deeper internalization of a male gender role. Overall, our data reveals the orientation-, but not identity-tuning of body-gender aftereffects and points to the association between alterations of the malleability of body gender perception and social deficits.

The emotional adaptation aftereffect discriminates between individuals with high and low levels of depressive symptoms.

The adaptation aftereffect plays a critical role in human development and survival. Existing studies have found that, compared with general individuals, individuals with learning disability, autism and dyslexia show a smaller amount of non-affective-based cognitive adaptation aftereffect. Nevertheless, it is unclear whether individuals with depression or depression tendency show similar phenomenon in the adaptation aftereffect, and whether such depression tendency occurs in the non-affective-based cognitive or emotional adaptation aftereffect. To address this question, the present study conducted two experiments. Experiments 1A and 1B used the emotional facial expression adaptation paradigm to examine whether Chinese participants showed the emotional adaptation aftereffect and whether the emotional adaptation aftereffect was influenced by physical features of faces, respectively. Experiment 2 recruited two groups of participants, with high and low depression, respectively, to examine whether they showed differences in the emotional or cognitive adaptation aftereffect. Results showed that Chinese participants showed the typical emotional adaptation aftereffect, which was not influenced by physical features of faces. More importantly, compared to the low-depression group, the high-depression group showed a smaller emotional adaptation aftereffect, but the two groups showed a similar cognitive adaptation aftereffect. These results suggest that level of depressive symptoms is associated with the emotional adaptation aftereffect.

Temporal enhancement of cross-adaptation between density and size perception based on the theory of magnitude.

The ability to estimate spatial extent is an important feature of the visual system. A previous study showed that perceived sizes of stimuli shrank after adaptation to a dense texture and that this density-size aftereffect was modulated by the degree of density. In this study, we found that the aftereffect was also modulated by the temporal density of the adapting texture. The test stimuli were two circles, and the adapting stimulus had a dotted texture. The adapting texture refreshed every 67 to 500 ms, or not at all (static), during the adaptation. The results showed that the aftereffects from a refreshing stimulus were larger than those under the static condition. On the other hand, density adaptation lacked such enhancement. This result indicates that repetitive presentation of an adapting texture enhanced the density-size cross-aftereffect. The fact that density modulation occurs in both the spatial and temporal domains is consistent with the theory of magnitude, which assumes that the processing of the magnitude estimation of space, time, and numbers share a common cortical basis.

Spontaneous recovery of adaptation aftereffects of natural facial categories.

Adaptation to a natural face attribute such as a happy face can bias the perception of a subsequent face in this dimension such as a neutral face. Such face adaptation aftereffects have been widely found in many natural facial categories. However, how temporally tuned mechanisms could control the temporal dynamics of natural face adaptation aftereffects remains unknown. To address the question, we used a deadaptation paradigm to examine whether the spontaneous recovery of natural facial aftereffects would emerge in four natural facial categories including variable categories (emotional expressions in Experiment 1 and eye gaze in Experiment 2) and invariable categories (facial gender in Experiment 3 and facial identity in Experiment 4). In the deadaptation paradigm, participants adapted to a face with an extreme attribute (such as a 100% angry face in Experiment 1) for a relatively long duration, and then deadapted to a face with an opposite extreme attribute (such as a 100% happy face in Experiment 1) for a relatively short duration. The time courses of face adaptation aftereffects were measured using a top-up manner. Deadaptation only masked the effects of initial longer-lasting adaptation, and the spontaneous recovery of adaptation aftereffects was observed at the post-test stage for all four natural facial categories. These results likely indicate that the temporal dynamics of adaptation aftereffects of natural facial categories may be controlled by multiple temporally tuned mechanisms.

The implied motion aftereffect changes decisions, but not confidence.

Viewing static images depicting movement can result in a motion aftereffect: people tend to categorise direction signals as moving in the opposite direction relative to the implied motion in still photographs. This finding could indicate that inferred motion direction can penetrate sensory processing and change perception. Equally possible, however, is that inferred motion changes decision processes, but not perception. Here we test these two possibilities. Since both categorical decisions and subjective confidence are informed by sensory information, confidence can be informative about whether an aftereffect probably results from changes to perceptual or decision processes. We therefore used subjective confidence as an additional measure of the implied motion aftereffect. In Experiment 1 (implied motion), we find support for decision-level changes only, with no change in subjective confidence. In Experiment 2 (real motion), we find equal changes to decisions and confidence. Our results suggest the implied motion aftereffect produces a bias in decision-making, but leaves perceptual processing unchanged.

Adaptation to one perceived motion direction can generate multiple velocity aftereffects.

Sensory adaptation is a useful tool to identify the links between perceptual effects and neural mechanisms. Even though motion adaptation is one of the earliest and most documented aftereffects, few studies have investigated the perception of direction and speed of the aftereffect at the same time, that is the perceived velocity. Using a novel experimental paradigm, we simultaneously recorded the perceived direction and speed of leftward or rightward moving random dots before and after adaptation. For the adapting stimulus, we chose a horizontally-oriented broadband grating moving upward behind a circular aperture. Because of the aperture problem, the interpretation of this stimulus is ambiguous, being consistent with multiple velocities, and yet it is systematically perceived as moving at a single direction and speed. Here we ask whether the visual system adapts to the multiple velocities of the adaptor or to just the single perceived velocity. Our results show a strong repulsion aftereffect, away from the adapting velocity (downward and slower), that increases gradually for faster test stimuli as long as these stimuli include some velocities that match some of the ambiguous ones of the adaptor. In summary, the visual system seems to adapt to the multiple velocities of an ambiguous stimulus even though a single velocity is perceived. Our findings can be well described by a computational model that assumes a joint encoding of direction and speed and that includes an extended adaptation component that can represent all the possible velocities of the ambiguous stimulus.

The McCollough World: Induction of orientation-contingent aftereffects with an altered-reality system.

The McCollough Effect is a color aftereffect produced by exposure to colored, oriented patterns. For example, following adaptation to vertical red and horizontal green stripes in alternation, vertical black and white patterns appear greenish, while horizontal black and white patterns appear reddish. The striking aspect of the McCollough Effect is that just a few minutes of adaptation can produce an aftereffect lasting days or weeks. Though this effect is easily induced, previous work has shown that stronger effects can be achieved with longer periods of adaptation. To allow especially long adaptation durations, the current work develops a novel method of induction of the McCollough Effect using live video feed, filtered by orientation, and viewed with a head-mounted display. Results showed that this "McCollough World" paradigm was as strong an inducer (per unit time) as traditional paradigms using gratings, while allowing observers to adapt comfortably for multiple hours. Two hours of McCollough World adaptation produced effects that were significantly larger than 20 min of traditional adaptation, which is close to the tolerance limits for gratings. This work provides insight into the features necessary for induction of the McCollough Effect and provides a strategy for creating especially strong and long-lasting color aftereffects.

Cross-modal motion aftereffects transfer between vision and touch in early deaf adults.

Previous research on early deafness has primarily focused on the behavioral and neural changes in the intact visual and tactile modalities. However, how early deafness changes the interplay of these two modalities is not well understood. In the current study, we investigated the effect of auditory deprivation on visuo-tactile interaction by measuring the cross-modal motion aftereffect. Consistent with previous findings, motion aftereffect transferred between vision and touch in a bidirectional manner in hearing participants. However, for deaf participants, the cross-modal transfer occurred only in the tactile-to-visual direction but not in the visual-to-tactile direction. This unidirectional cross-modal motion aftereffect found in the deaf participants could not be explained by unisensory motion aftereffect or discrimination threshold. The results suggest a reduced visual influence on tactile motion perception in early deaf individuals.

Stronger tilt aftereffects in persons with schizophrenia.

Individuals with schizophrenia may fail to appropriately use temporal context and apply past environmental regularities to the interpretation of incoming sensory information. Here we use the visual system as a test bed for investigating how prior experience shapes perception in individuals with schizophrenia. Specifically, we use visual aftereffects, illusory percepts resulting from prior exposure to visual input, to measure the influence of prior events on current processing. At a neural level, visual aftereffects arise due to attenuation in the responses of neurons that code the features of the prior stimulus (neuronal adaptation) and subsequent disinhibition of neurons signaling activity at the opposite end of the feature dimension. In the current study, we measured tilt aftereffects and negative afterimages, 2 types of aftereffects that reflect, respectively, adaptation of cortical orientation-coding neurons and adaptation of subcortical and retinal luminance-coding cells in persons with schizophrenia (PSZ; n = 36) and demographically matched healthy controls (HC; n = 22). We observed stronger tilt aftereffects in PSZ compared to HC, but no difference in negative afterimages. Stronger tilt aftereffects were related to more severe negative symptoms. These data suggest oversensitivity to recent regularities, in the form of stronger visual adaptation, at cortical, but not subcortical, levels in schizophrenia. (PsycInfo Database Record (c) 2021 APA, all rights reserved).

Motion-form interaction: Motion and form aftereffects induced by distorted static natural scenes.

Spatially varying distortions (SVDs) are common artifacts of spectacles like progressive additional lenses (PALs). To habituate to distortions of PALs, the visual system has to adapt to distortion-induced image alterations, termed skew adaptation. But how this visual adjustment is achieved is largely unknown. This study examines the properties of visual adaptation to distortions of PALs in natural scenes. The visual adaptation in response to altered form and motion features of the natural stimuli were probed in two different psychophysical experiments. Observers were exposed to distortions in natural images, and form and motion aftereffects were tested subsequently in a constant stimuli procedure where subjects were asked to judge the skew, or the motion direction of an according test stimulus. Exposure to skewed natural stimuli induced a shift in perceived undistorted form as well as motion direction, when viewing distorted dynamic natural scenes, and also after exposure to static distorted natural images. Therefore, skew adaptation occurred in form and motion for dynamic visual scenes as well as static images. Thus, specifically in the condition of static skewed images and the test feature of motion direction, cortical interactions between motion-form processing presumably contributed to the adaptation process. In a nutshell, interfeature cortical interactions constituted the adaptation process to distortion of PALs. Thus, comprehensive investigation of adaptation to distortions of PALs would benefit from taking into account content richness of the stimuli to be used, like natural images.

Number Adaptation Can Be Dissociated From Density Adaptation.

Rapidly judging the number of objects in a scene is an important perceptual ability. Recent debates have centered on whether number perception is accomplished by dedicated mechanisms and, in particular, on whether number-adaptation aftereffects reflect adaptation of number per se or adaptation of related stimulus properties, such as density. Here, we report an adaptation experiment (N = 8) for which the predictions of number and density theories are diametrically opposed. We found that when a reference stimulus has higher density than an adaptation stimulus but contains fewer elements, adaptation reduces the perceived number of elements in the reference stimulus. This is consistent with number adaptation and inconsistent with density adaptation. Thus, number-adaptation aftereffects are more than a by-product of density adaptation: When density and number are dissociated, adaptation effects are in the direction predicted by adaptation to number, not density.